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70 protocols using arm200cf

1

Characterization of REBCO Superconductor

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The 4.2 K and high field four-probe critical current Ic measurements were performed on ∼1 × 10 mm bridges in a 52 mm warm bore 31 T Bitter magnet fitted with a 38 mm bore liquid He cryostat at the National High Magnetic Field Laboratory (NHMFL). The local current distribution was characterized by magneto-optical imaging on a sample with ~7 mm wide and ~8 mm long. To assess the current blocking effects of the potential second phase particles and the microstructure homogeneity, back-scattered electron imaging was conducted in a Zeiss 1540EsB scanning electron microscope (SEM). TEM was carried out in a JEOL ARM200cF to examine the size and distribution of the pinning defects. The phase identification and texture analysis were conducted using θ-2θ measurements in a Siemens D5000 x-ray powder diffractometer and an area detector in Bruker general area detector diffraction system. The thickness of REBCO layer, ∼3.2 μm was determined from the cross-section SEM images prepared by focused ion beam milling.
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2

Phase Imaging of Gold Nanorods

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Holograms of AuNRs on the pure ultrathin (5 nm) silicon grid were acquired using the JEOL ARM 200CF, as described above, operated at 200 kV equipped with a biprism. Phase images were reconstructed using custom Gatan DigitalMicrograph scripts written by M. R. McCartney, Arizona State University (source code is available on request). The phase profiles presented in Fig. 2 (B and D) were calculated in Gatan DigitalMicrograph using the line profile tool.
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3

EELS Analysis of Nanomaterials

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EELS analysis was performed using a Gatan Quantum GIF965 dual EELS spectrometer attached to the transmission electron microscope (JEOL ARM-200CF) equipped with a cold field-emission electron gun and probe spherical-aberration corrector.
Reference materials used to maintain a traceability of specimen was NiO which has been traditionally used by EELS manufacturer. The samples had been kept uncontaminated, and carbon contamination was removed before and/or during the measurement. The measurement mode is STEM mode or diffraction mode. After checking the degree of carbon contamination and oxidation, in dual EELS mode, acquisition of EELS data was repeated five times in different locations and their average values of on-set energy were used. Then, the data was evaluated in accordance with the SR data evaluation procedures established by our data center. Detailed procedures and explanations will be mentioned in another paper.
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4

Atomic Structure Characterization of SrCoO2.5-σ Thin Films

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The atomic structures of the SrCoO2.5−σ films was characterized using an ARM—200CF (JEOL, Tokyo, Japan) transmission electron microscope operated at 200 kV and equipped with double spherical aberration (Cs) correctors. The attainable resolution of the probe defined by the objective pre-field is 78 picometers. ABF and HAADF images were acquired at acceptance angles of 11–22 and 90–250 mrad, respectively. All of the images presented here are Fourier-filtered to minimize the effect of the contrast noise. The filtering does not have any effect on the results of our measurements. In addition, we adjusted deliberately the brightness and contrast in order to better representation of the atomic arrangements, this adjustment does not have any effect on the result. The EELS experiments were carried out with a Gatan spectrometer attached to the TEM in the STEM mode operating at 200 kV. The convergence semi-angle for the electron probe was 22 mrad. The spectrometer was set to an energy dispersion of 0.25 eV/channel. All of the spectra were acquired with a short exposure time, which was as short as 0.05 s, in a line-scan manner. Three hundred spectra were summed to avoid electron beam damage.
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5

Structural Characterization of Superlattices

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High‐resolution XRD measurements were performed using a Rigaku Smartlab and a PANalytical X'Pert XRD. Atomic‐scale imaging of SLs was performed on a spherical aberration‐corrected scanning transmission electron microscope (STEM; ARM200CF, JEOL) operating at 200 kV. To detect the β‐dependency of octahedral distortions in SRO layers, the annular bright‐field (ABF) imaging mode was employed along with the high‐angle annular dark‐field (HAADF) imaging mode. The incident electron probe angle was set to 23 mrad, giving rise to a probe size of 0.78 Å. The ABF and HAADF signals were simultaneously collected over detector angle ranges of 7.5–17 and 70–175 mrad, respectively. Cross‐sectional thin samples for STEM analysis were prepared using a dual‐beam focused ion beam system (FIB, FEI Helios Nano Lab 450); subsequently, low‐energy Ar ion milling at 700 V (Fischione Model 1040, Nanomill) was carried out for 15 min to remove surface layers damaged owing to heavy Ga ion beam milling in the FIB system.
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6

Comprehensive Materials Characterization Protocol

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The XRD profile for each sample was collected using MiniFlexII (Rigaku Co. Ltd.) at room temperature. Monochromatic X-rays of Cu Kα radiation (λ = 0.154 nm) at 30 kV and 15 mA was applied. The observations of HR-TEM and STEM images were collected by ARM-200CF (JEOL, Ltd.) at an accelerated voltage of 120 kV. The sample was dispersed in highly purified hexane followed by dropping on a Cu mesh covered with carbon membranes (NS-C15, Okenshoji Co., Ltd.). TG profiles were obtained using Thermo plus EVO2 (Rigaku Co. Ltd.) under atmospheric conditions. In a typical TG experiment, ∼4 mg of a sample was placed in a Pt pan, and measurements were performed at a ramping rate of 10 K min−1 from room temperature to 1173 K. Moreover, XPS measurements were conducted using JEOL JPS-9030. The spectra were analysed with JEOL SpecSurf systems to deconvolute and analyse the bands. N2 adsorption–desorption isotherms at 77 K and Ar isotherms at 87 K on p-BN and AC were then measured using BELSORP-max (MicrotracBEL Corp.), and all samples were evacuated at 823 K at <1 mPa for 6 h.
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7

Bilayer WSe2 Characterization via AFM, Raman, PL, STEM

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AFM analysis was conducted on an atomic force microscope (AFM, Icon Bruker) equipped with a probe with a tip radius of <10 nm (TAP300AI-G, Budgetsensors) to evaluate the height profiles of bilayer WSe2. Raman and PL spectroscopy were performed under ambient conditions using an ND-MDT spectrometer equipped with a laser excitation wavelength of 532 nm. For STEM imaging, bilayer WSe2 flakes were transferred onto a holy-carbon TEM grid using a poly(methyl methacrylate) (PMMA)-assisted transfer process.58 (link) STEM was performed with a JEOL ARM 200CF equipped with a CEOS corrector (Cs ~ 100 nm) operating at 80 kV to reduce knock-on damage. Images were acquired with a HAADF detector from 54–220 mrad and cleaned using an average background subtraction filter (ABSF) SAED patterns were acquired with a JEOL F200 TEM operating at 200 kV using a selected-area aperture with an effective size at the sample of ~1 μm.
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8

Comprehensive Material Characterization Protocol

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X-ray diffraction (XRD) patterns were measured by a Shimadzu LabX XRD-6000 diffractometer with Cu kα radiation (λ = 0.15406 nm). Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses were performed on a Hitachi S-4800 microscope and an FEI-Tecnai G2 20 microscope, respectively. XPS measurements were conducted by using a VG ESCALAB 250 instrument with a monochromatized Al X-ray source (1486.6 eV). Nitrogen adsorption–desorption isotherms were obtained from a Quadrasorb instrument at 77 K. ICP-AES was detected by a Perinlmer Optima 2000DV instrument. The HAADF-STEM images were obtained on a JEOL ARM200CF fifth order aberration-corrected TEM equipped with a dual-type EDS detector. The X-ray absorption find structure spectra were measured at the BL8C beamline in Pohang Light Source (PLS), Korea.
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9

Characterization of Nanomaterials by TEM-EDX

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Transmission electron microscopy (TEM) was
performed on a JEOL JEM-2100 operating at 200 kV. Energy dispersive
X-ray analysis (EDX) was done using an Oxford Instruments X-MaxN 80
detector, and the data were analyzed using the Aztec software. Samples
were prepared by dispersion in ethanol by sonication and deposited
on 300-mesh copper grids coated with a holey carbon film. High angle
annular dark-field (HAADF) scanning transmission electron microscopy
(STEM) imaging was done using a JEOL ARM200CF operating at 200 kV.
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10

Thin Film Growth and Characterization

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Thirty-five–nanometer SCO and 17-nm SRO thin films were grown on a STO (001) and STO (110) substrate by using a reflection high-energy electron diffraction–assisted PLD system. The growth conditions were optimized at the temperature of 750°C with an oxygen environment of 100 mtorr. The laser energy (KrF, λ = 248 nm) was fixed at 1.2 J/cm2 with the repetition rate of 2 Hz. After the film growth, the samples were cooled down to room temperature at the cooling rate of 7°C/min in the oxygen atmosphere of 100 mtorr. Each sample thickness was controlled by the growth time, and the crystalline structures of the thin films were characterized by XRD and reciprocal space mapping. The atomic structures of the SCO films were characterized using an ARM 200CF (JEOL, Tokyo, Japan) transmission electron microscope.
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